BDBM50120296 CHEMBL419918::Peptide Boronic Acid analogue

SMILES: CC[C@H](NC(=O)[C@H]1CCCN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)B1O[C@@H]2C[C@@H]3C[C@@H](C3(C)C)[C@]2(C)O1

InChI Key: InChIKey=WPOOMCSSVQWZRO-RCXOJNRVSA-N

Data: 1 KI  2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50120296   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Hepatitis C virus serine protease, NS3/NS4A (Hepatitis C virus)	BDBM50120296 (CHEMBL419918 | Peptide Boronic Acid analogue) Show SMILES CC[C@H](NC(=O)[C@H]1CCCN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)B1O[C@@H]2C[C@@H]3C[C@@H](C3(C)C)[C@]2(C)O1 Show InChI InChI=1S/C37H61BN6O11/c1-9-26(38-54-25-16-20-15-24(36(20,6)7)37(25,8)55-38)41-33(51)23-11-10-14-44(23)35(53)30(19(4)5)43-34(52)29(18(2)3)42-32(50)22(12-13-27(45)46)40-31(49)21(39)17-28(47)48/h18-26,29-30H,9-17,39H2,1-8H3,(H,40,49)(H,41,51)(H,42,50)(H,43,52)(H,45,46)(H,47,48)/t20-,21-,22-,23+,24-,25+,26-,29-,30-,37-/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Binding affinity against Hepatitis C virus NS3 protease				Bioorg Med Chem Lett 12: 3199-202 (2002) BindingDB Entry DOI: 10.7270/Q2R49Q38
					More data for this Ligand-Target Pair
Leukocyte elastase (Homo sapiens (Human))	BDBM50120296 (CHEMBL419918 | Peptide Boronic Acid analogue) Show SMILES CC[C@H](NC(=O)[C@H]1CCCN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)B1O[C@@H]2C[C@@H]3C[C@@H](C3(C)C)[C@]2(C)O1 Show InChI InChI=1S/C37H61BN6O11/c1-9-26(38-54-25-16-20-15-24(36(20,6)7)37(25,8)55-38)41-33(51)23-11-10-14-44(23)35(53)30(19(4)5)43-34(52)29(18(2)3)42-32(50)22(12-13-27(45)46)40-31(49)21(39)17-28(47)48/h18-26,29-30H,9-17,39H2,1-8H3,(H,40,49)(H,41,51)(H,42,50)(H,43,52)(H,45,46)(H,47,48)/t20-,21-,22-,23+,24-,25+,26-,29-,30-,37-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Inhibitory concentration against Human leukocyte Elastase				Bioorg Med Chem Lett 12: 3199-202 (2002) BindingDB Entry DOI: 10.7270/Q2R49Q38
					More data for this Ligand-Target Pair
Chymotrypsin (Homo sapiens (Human))	BDBM50120296 (CHEMBL419918 | Peptide Boronic Acid analogue) Show SMILES CC[C@H](NC(=O)[C@H]1CCCN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)B1O[C@@H]2C[C@@H]3C[C@@H](C3(C)C)[C@]2(C)O1 Show InChI InChI=1S/C37H61BN6O11/c1-9-26(38-54-25-16-20-15-24(36(20,6)7)37(25,8)55-38)41-33(51)23-11-10-14-44(23)35(53)30(19(4)5)43-34(52)29(18(2)3)42-32(50)22(12-13-27(45)46)40-31(49)21(39)17-28(47)48/h18-26,29-30H,9-17,39H2,1-8H3,(H,40,49)(H,41,51)(H,42,50)(H,43,52)(H,45,46)(H,47,48)/t20-,21-,22-,23+,24-,25+,26-,29-,30-,37-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Inhibitory concentration against Human pancreatic Serine protease chymotrypsin				Bioorg Med Chem Lett 12: 3199-202 (2002) BindingDB Entry DOI: 10.7270/Q2R49Q38
					More data for this Ligand-Target Pair